Whether you are familiar with the production part approval process (PPAP) requirement, need a refresher or are new to PPAP altogether, this overview course is for you.
Become versed on the procedures, reporting requirements and activities specified by the PPAP manual. Instruction covers the fourth edition manual, submission and specific requirements for part approval records/sample retention, and part-submission status. A review of forms in the PPAP manual is also included.
Who Should Attend
Recommended for mechanical engineers, manufacturing engineers, quality engineers, PPAP coordinators, project and program managers, quality managers and quality team leaders, ISO/TS 16949 internal auditors, second-party auditors, anyone involved in product quality planning activities, anyone interested in learning more about APQP, and anyone involved in the implementation of ISO/TS 16949 and anyone who wants a better understanding of the quality planning process.
- Discuss and evaluate the procedures, reporting requirements and activities specified by the PPAP manual
- Review and discuss the PPAP forms
- Explain submission and specific requirements for part approval records/sample retention
Please Note: Attendance to the entire course is required to receive a Certificate of Attendance